Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name gas, calibration (specified concentration)
510(k) Number K932520
Device Name CALIBRATION GAS
Applicant
CRYODYNE TECHNOLOGIES, INC.
67 WINTHROP RD.
CHESTER,  CT  06412
Applicant Contact VINCENT J TOILO
Correspondent
CRYODYNE TECHNOLOGIES, INC.
67 WINTHROP RD.
CHESTER,  CT  06412
Correspondent Contact VINCENT J TOILO
Regulation Number868.6400
Classification Product Code
BXK  
Date Received05/25/1993
Decision Date 08/19/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-